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Pleiotropic effects of the CD30 ligand on CD30-expressing cells and
lymphoma cell lines
HJ Gruss, N Boiani, DE Williams, RJ Armitage, CA Smith and RG Goodwin
Immunex Research and Development Corp, Department of Biochemistry, Seattle,
WA 98101.
CD30 is a member of the tumor necrosis factor receptor superfamily. CD30
was originally described as a cell surface antigen on primary and cultured
Hodgkin's and Reed-Sternberg cells. In this study, recombinant human CD30
ligand was expressed on the surface of CV-1/EBNA cells and tested for
biologic activities on a variety of different CD30+ human lymphoma cell
lines. CD30 ligand enhanced Ig secretion of Epstein-Barr virus
(EBV)-immortalized, CD30+ lymphoblastoid B-cell lines, but not Burkitt
lymphoma lines. Recombinant CD30 ligand enhanced proliferation of
"T-cell-like" Hodgkin's disease-derived cell lines and an adult T- cell
leukemia cell line, but not "B-cell-like" Hodgkin's disease- derived cell
lines, CD30+, EBV-immortalized lymphoblastoid B-cell lines, or CD30+ and
EBV+ tumor B-cell non-Hodgkin's lymphoma cell lines. In addition, CD30
ligand mediated reduction of proliferation and viability, by induction of
cytolytic cell death, of CD30+, large-cell anaplastic lymphoma cell lines.
Two new antibodies, M44 and M67, against the CD30 antigen demonstrated
similar biologic activities to the CD30 ligand. Taken together, these data
demonstrate pleiotropic biologic activities of the CD30 ligand on different
CD30+ lymphoma cell lines and indicate that the CD30-CD30 ligand
interaction might have a pathophysiologic role in Hodgkin's and some
non-Hodgkin's lymphomas.
Volume 83,
Issue 8,
pp. 2045-2056,
04/15/1994
Copyright © 1994 by The American Society of Hematology

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